Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812868C= , CM000664.2:g.218812868C= | GRCh38 |
| NC_000002.11:g.219677591C= , CM000664.1:g.219677591C= | GRCh37 |
| NC_000002.10:g.219385835C= | NCBI36 |
| NG_007959.1:g.36120C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.845-56C= MANE Select | ENSP00000258415.4:n.845-56C= | |
| ENST00000258415.8:c.845-56C= | ENSP00000258415.4:n.845-56C= | |
| ENST00000411688.1:c.563-56C= | ENSP00000392671.1:n.563-56C= | |
| ENST00000445971.1:c.*306-56C= | ENSP00000404945.1:n.*306-56C= | |
| ENST00000466602.1:n.911C= | ||
| ENST00000494263.5:n.1279-56C= | ||
| NM_000784.3:c.845-56C= | NP_000775.1:n.845-56C= | |
| XM_017003488.2:c.425-56C= | XP_016858977.1:n.425-56C= | |
| NM_000784.4:c.845-56C= MANE Select | NP_000775.1:n.845-56C= |